Canonical Allele Identifier: CA399478967
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584413C>A , CM000679.2:g.41584413C>A GRCh38
NC_000017.10:g.39740665C>A , CM000679.1:g.39740665C>A GRCh37
NC_000017.9:g.36994191C>A NCBI36
NG_008624.1:g.7483G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609G>T MANE Select ENSP00000167586.6:p.Lys203Asn
ENST00000167586.6:c.609G>T ENSP00000167586.6:p.Lys203Asn
ENST00000476662.1:n.59G>T
NM_000526.4:c.609G>T NP_000517.2:p.Lys203Asn
NM_000526.5:c.609G>T MANE Select NP_000517.3:p.Lys203Asn